1)  chlorophyll α
叶绿素α浓度
1.
Investigations of chlorophyll α was carried out in the seawater and sediment in the Chukchi Sea, Chukchi Plateau, the Slop-flow area, the Mendeleev Ride and the Canada Basin during the 2nd Chinese National Arctic Research Expedition in the summer of 2003.
结果表明,观测水体叶绿素α浓度变化范围为0。
2)  leaf green ;foliage green
叶绿
3)  chlorophyll-a
叶绿素a
1.
Mutlianalysis between chlorophyll-a and environmental factors in Dianshan Lake water;
淀山湖水体叶绿素a与水质因子的多元分析
2.
Inversion of chlorophyll-a concentration in turbid water of Lake Taihu based on optimized multi-spectral combination;
基于半分析模型的波段最优化组合反演混浊太湖水体叶绿素a
3.
Multi-analysis of Chlorophyll-a and Environmental Factors in a Surface Water Source in Zhengzhou, China;
郑州市某地表水源叶绿素a与相关环境因子的关系
4)  chlorophyll
叶绿素
1.
Study on stability of chlorophyll from Corydalis;
紫堇叶绿素稳定性的研究
2.
Study on the optimum extraction condition of the chlorophyll from ulva pertusa;
绿藻石莼叶绿素提取工艺的研究
3.
Prediction of broccoli chlorophyll change during storage by difference method;
差分法预测稳态贮藏条件下嫩茎花椰菜中叶绿素的变化
5)  Chl-a
叶绿素a
1.
Effect of hydroxyl on chl-a in algae cells;
羟基对海洋微藻细胞叶绿素a的影响
2.
Distribution characteristics and influenced factors of Chl-a in Beihai Bay;
北海湾叶绿素a的分布特征及其影响因素
3.
The algal biomass was measured daily; its Chl-a content, the amount of Mn adsorbed on an algal and its Mn content were measured at the end of the test runs.
结果表明,Mn2+为0mg/L时,铜绿微囊藻生长受到很大抑制,叶绿素a含量较低;Mn2+为0。
6)  Chlorophyll a
叶绿素a
1.
Transient Absorption of the Chlorophyll a in Ethanol;
叶绿素a分子在乙醇溶剂中的瞬态吸收研究(英文)
2.
Discussing about chlorophyll a determination method in fresh water;
淡水中叶绿素a测定方法的探讨
3.
Spatial-temporal distribution of chlorophyll a in the Zhelin Bay——A large-scale maricultural area;
大规模增养殖区柘林湾叶绿素a的时空分布
参考词条
补充资料：α,α,α,α',α',α'-六氯对二甲苯
分子式：C8H4Cl6
分子量：312.84
CAS号：68-36-0

性质：白色针状或粉末状结晶。熔点108-110℃。溶于二甲苯、石油醚、乙醇、植物油，不溶于水。无味，有特殊臭味，遇光、碱会缓慢分解而呈酸性。

制备方法：以混二甲苯为原料，先用98%硫酸磺化，使间二甲苯生成间二甲苯磺酸盐。从磺化反应物中分离出含邻、对二甲苯的油层，水洗、干燥，减压蒸馏出邻、对二甲苯。间二甲苯磺酸盐经水解可得副产品间二甲苯。由邻、对二甲苯经氯化即得1，4-双（三氯甲基）苯：在反应锅中投入邻、对二甲苯，再加入过氧化苯甲酰和三乙醇胺。加热到70℃后，在光照射下导入氯气，于70-80℃反应6h，再升温至100-120℃继续反应，至反应液相对密度达到1.560-1.580（65℃），即为反应终点，停止通氯，减压脱除余氯。降温至5℃，过滤，洗涤得粗品，重结晶，活性炭脱色得成品。

用途：抗血吸虫病药物。对肝吸虫病、阿米巴原虫病、疟疾以及肠道线虫有一定疗效。但对神经系统的不良反应较多见，且延迟反应持续较久。

说明：补充资料仅用于学习参考，请勿用于其它任何用途。